cutaneous t cell lymphoma |
Disease ID | 846 |
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Disease | cutaneous t cell lymphoma |
Definition | A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders. |
Synonym | cells cutaneous lymphomas t ctcl ctcl - cutaneous t-cell lymphoma cutaneous t-cell lymphoma cutaneous t-cell lymphoma (morphologic abnormality) cutaneous t-cell lymphoma, no icd-o subtype cutaneous t-cell lymphoma, no icd-o subtype (morphologic abnormality) cutaneous t-cell lymphoma, no international classification of diseases for oncology subtype cutaneous t-cell lymphoma, no international classification of diseases for oncology subtype (morphologic abnormality) cutaneous t-cell lymphomas cutaneous t-cell non-hodgkin lymphoma cutaneous t-cell non-hodgkin's lymphoma lymphoma, cutaneous t-cell lymphoma, t cell, cutaneous lymphoma, t-cell, cutaneous lymphoma, t-cell, cutaneous [disease/finding] lymphomas, cutaneous t-cell primary cutaneous t-cell lymphoma primary cutaneous t-cell lymphoma (disorder) primary cutaneous t-cell non-hodgkin's lymphoma skin t-cell non-hodgkin's lymphoma t cell cutaneous lymphoma t cell lymphoma, cutaneous t-cell cutaneous lymphoma t-cell lymphoma, cutaneous t-cell lymphomas, cutaneous t-cell non-hodgkin's lymphoma of skin t-cell non-hodgkin's lymphoma of the skin |
Orphanet | |
DOID | |
UMLS | C0079773 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:25) C0026948 | mycosis fungoides | 9 C0026946 | mycosis | 8 C0036920 | sezary syndrome | 3 C0024299 | lymphoma | 2 C0004623 | bacterial infections | 2 C0004623 | bacterial infection | 2 C0018801 | heart failure | 1 C0019829 | hodgkin's disease | 1 C0040053 | thrombus | 1 C0024314 | lymphoproliferative disorders | 1 C0023434 | chronic lymphocytic leukemia | 1 C0085110 | severe combined immunodefic | 1 C0263505 | alopecia universalis | 1 C0030326 | panniculitis | 1 C0015645 | fasciitis | 1 C0042900 | vitiligo | 1 C0026764 | myeloma | 1 C0037274 | skin disorder | 1 C0002170 | alopecia | 1 C0037274 | skin disorders | 1 C0079773 | cutaneous t-cell lymphoma | 1 C0023448 | lymphocytic leukemia | 1 C0033860 | psoriasis | 1 C0024314 | lymphoproliferative disorder | 1 C0018802 | congestive heart failure | 1 |
Curated Gene | Entrez_id | Symbol | Resource(Total Genes:21) 673 | BRAF | CTD_human 7128 | TNFAIP3 | CTD_human 1493 | CTLA4 | CTD_human 7157 | TP53 | CTD_human 4170 | MCL1 | CTD_human 8289 | ARID1A | CTD_human 5335 | PLCG1 | CTD_human 6935 | ZEB1 | CTD_human 1029 | CDKN2A | CTD_human 6777 | STAT5B | CTD_human 1788 | DNMT3A | CTD_human 472 | ATM | CTD_human 10664 | CTCF | CTD_human 3662 | IRF4 | CTD_human 581 | BAX | CTD_human 84433 | CARD11 | CTD_human 355 | FAS | CTD_human 387 | RHOA | CTD_human 4791 | NFKB2 | CTD_human 940 | CD28 | CTD_human 5588 | PRKCQ | CTD_human |
Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:23) 1906 | EDN1 | CIPHER 3569 | IL6 | CIPHER 4170 | MCL1 | CTD_human 7157 | TP53 | CTD_human 6777 | STAT5B | CTD_human 1788 | DNMT3A | CTD_human 7128 | TNFAIP3 | CTD_human 1493 | CTLA4 | CTD_human 4791 | NFKB2 | CTD_human 5588 | PRKCQ | CTD_human 940 | CD28 | CTD_human 355 | FAS | CTD_human 6935 | ZEB1 | CTD_human 581 | BAX | CTD_human 1029 | CDKN2A | CTD_human 84433 | CARD11 | CTD_human 472 | ATM | CTD_human 387 | RHOA | CTD_human 3662 | IRF4 | CTD_human 673 | BRAF | CTD_human 10664 | CTCF | CTD_human 8289 | ARID1A | CTD_human 5335 | PLCG1 | CTD_human |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:167) 100 | ADA | 1.715 | DISEASES 55811 | ADCY10 | 1.142 | DISEASES 51390 | AIG1 | 2.426 | DISEASES 238 | ALK | 3.248 | DISEASES 51378 | ANGPT4 | 1.205 | DISEASES 64225 | ATL2 | 1.29 | DISEASES 567 | B2M | 2.141 | DISEASES 64919 | BCL11B | 1.483 | DISEASES 10018 | BCL2L11 | 1.523 | DISEASES 605 | BCL7A | 3.067 | DISEASES 65980 | BRD9 | 1.572 | DISEASES 79886 | CAAP1 | 1.472 | DISEASES 147968 | CAPN12 | 2.385 | DISEASES 84433 | CARD11 | 2.19 | DISEASES 841 | CASP8 | 1.096 | DISEASES 25901 | CCDC28A | 2.109 | DISEASES 80323 | CCDC68 | 1.846 | DISEASES 6364 | CCL20 | 1.585 | DISEASES 1232 | CCR3 | 2.435 | DISEASES 1233 | CCR4 | 1.896 | DISEASES 1237 | CCR8 | 1.345 | DISEASES 9332 | CD163 | 2.197 | DISEASES 930 | CD19 | 1.632 | DISEASES 914 | CD2 | 4.734 | DISEASES 50489 | CD207 | 2.291 | DISEASES 29126 | CD274 | 1.187 | DISEASES 958 | CD40 | 1.059 | DISEASES 959 | CD40LG | 2.647 | DISEASES 921 | CD5 | 4.622 | DISEASES 1043 | CD52 | 4.1 | DISEASES 9308 | CD83 | 2.014 | DISEASES 942 | CD86 | 1.681 | DISEASES 1029 | CDKN2A | 2.123 | DISEASES 1107 | CHD3 | 1.267 | DISEASES 170482 | CLEC4C | 1.269 | DISEASES 1452 | CSNK1A1 | 1.012 | DISEASES 1485 | CTAG1B | 1.055 | DISEASES 64693 | CTAGE1 | 2.197 | DISEASES 6387 | CXCL12 | 1.311 | DISEASES 284340 | CXCL17 | 1.717 | DISEASES 4283 | CXCL9 | 1.848 | DISEASES 2833 | CXCR3 | 3.194 | DISEASES 26052 | DNM3 | 2.229 | DISEASES 1791 | DNTT | 1.463 | DISEASES 1803 | DPP4 | 3.569 | DISEASES 56940 | DUSP22 | 2.636 | DISEASES 10938 | EHD1 | 1.626 | DISEASES 8667 | EIF3H | 1.29 | DISEASES 30816 | ERVW-1 | 2.976 | DISEASES 355 | FAS | 2.803 | DISEASES 100302740 | FAS-AS1 | 1.679 | DISEASES 356 | FASLG | 2.433 | DISEASES 2214 | FCGR3A | 2.417 | DISEASES 115352 | FCRL3 | 2.017 | DISEASES 344018 | FIGLA | 1.824 | DISEASES 50943 | FOXP3 | 3.442 | DISEASES 6624 | FSCN1 | 1.071 | DISEASES 2526 | FUT4 | 2.247 | DISEASES 2625 | GATA3 | 2.023 | DISEASES 115362 | GBP5 | 1.766 | DISEASES 7107 | GPR137B | 2.2 | DISEASES 3065 | HDAC1 | 3.029 | DISEASES 3066 | HDAC2 | 2.388 | DISEASES 10013 | HDAC6 | 2.571 | DISEASES 55869 | HDAC8 | 1.76 | DISEASES 9734 | HDAC9 | 1.638 | DISEASES 51696 | HECA | 3.907 | DISEASES 3320 | HSP90AA1 | 1.219 | DISEASES 3384 | ICAM2 | 1.211 | DISEASES 3430 | IFI35 | 1.511 | DISEASES 3440 | IFNA2 | 2.3 | DISEASES 338376 | IFNE | 1.164 | DISEASES 147920 | IGFL2 | 2.645 | DISEASES 3550 | IK | 1.222 | DISEASES 3586 | IL10 | 2.903 | DISEASES 3605 | IL17A | 2.022 | DISEASES 112744 | IL17F | 2.287 | DISEASES 3559 | IL2RA | 2.988 | DISEASES 3561 | IL2RG | 2.757 | DISEASES 386653 | IL31 | 3.411 | DISEASES 133396 | IL31RA | 2.178 | DISEASES 9235 | IL32 | 2.132 | DISEASES 3662 | IRF4 | 2.062 | DISEASES 3664 | IRF6 | 1.288 | DISEASES 3676 | ITGA4 | 2.155 | DISEASES 3683 | ITGAL | 1.805 | DISEASES 3684 | ITGAM | 1.352 | DISEASES 3716 | JAK1 | 1.877 | DISEASES 3718 | JAK3 | 3.691 | DISEASES 3802 | KIR2DL1 | 2.557 | DISEASES 3804 | KIR2DL3 | 2.521 | DISEASES 3811 | KIR3DL1 | 4.171 | DISEASES 3812 | KIR3DL2 | 5.638 | DISEASES 3824 | KLRD1 | 1.449 | DISEASES 3909 | LAMA3 | 1.117 | DISEASES 54900 | LAX1 | 2.334 | DISEASES 3932 | LCK | 1.734 | DISEASES 84946 | LTV1 | 1.781 | DISEASES 51213 | LUZP4 | 1.325 | DISEASES 4111 | MAGEA12 | 1.063 | DISEASES 4216 | MAP3K4 | 1.329 | DISEASES 4170 | MCL1 | 1.013 | DISEASES 4193 | MDM2 | 1.036 | DISEASES 2315 | MLANA | 1.127 | DISEASES 4311 | MME | 2.467 | DISEASES 4507 | MTAP | 1.858 | DISEASES 10608 | MXD4 | 1.327 | DISEASES 4601 | MXI1 | 1.691 | DISEASES 4602 | MYB | 1.146 | DISEASES 4609 | MYC | 2.621 | DISEASES 26292 | MYCBP | 1.398 | DISEASES 89795 | NAV3 | 3.914 | DISEASES 9436 | NCR2 | 1.281 | DISEASES 259197 | NCR3 | 1.026 | DISEASES 4791 | NFKB2 | 1.056 | DISEASES 4942 | OAT | 3.366 | DISEASES 56666 | PANX2 | 1.211 | DISEASES 142 | PARP1 | 1.098 | DISEASES 5079 | PAX5 | 1.826 | DISEASES 5358 | PLS3 | 4.7 | DISEASES 5406 | PNLIP | 1.969 | DISEASES 10631 | POSTN | 1.081 | DISEASES 5527 | PPP2R5C | 1.512 | DISEASES 5728 | PTEN | 1.32 | DISEASES 5788 | PTPRC | 3.339 | DISEASES 5793 | PTPRG | 1.005 | DISEASES 5887 | RAD23B | 2.047 | DISEASES 63891 | RNF123 | 1.895 | DISEASES 9349 | RPL23 | 1.441 | DISEASES 6257 | RXRB | 1.011 | DISEASES 6278 | S100A7 | 1.055 | DISEASES 6280 | S100A9 | 1.805 | DISEASES 6304 | SATB1 | 2.537 | DISEASES 6401 | SELE | 2.12 | DISEASES 259230 | SGMS1 | 1.453 | DISEASES 140885 | SIRPA | 1.063 | DISEASES 8631 | SKAP1 | 1.667 | DISEASES 23583 | SMUG1 | 1.336 | DISEASES 100126781 | SNAR-F | 1.342 | DISEASES 26801 | SNORD48 | 1.139 | DISEASES 6693 | SPN | 3.254 | DISEASES 23626 | SPO11 | 1.372 | DISEASES 6772 | STAT1 | 1.791 | DISEASES 6775 | STAT4 | 2.995 | DISEASES 6776 | STAT5A | 3.514 | DISEASES 6847 | SYCP1 | 2.415 | DISEASES 6863 | TAC1 | 1.534 | DISEASES 7062 | TCHH | 1.05 | DISEASES 7037 | TFRC | 1.671 | DISEASES 387357 | THEMIS | 2.57 | DISEASES 7072 | TIA1 | 4.327 | DISEASES 201633 | TIGIT | 1.017 | DISEASES 51284 | TLR7 | 1.463 | DISEASES 54106 | TLR9 | 1.445 | DISEASES 253582 | TMEM244 | 2.965 | DISEASES 7110 | TMF1 | 3.749 | DISEASES 7124 | TNF | 2.304 | DISEASES 8764 | TNFRSF14 | 1.203 | DISEASES 7133 | TNFRSF1B | 1.496 | DISEASES 7293 | TNFRSF4 | 1.647 | DISEASES 9760 | TOX | 3.983 | DISEASES 80342 | TRAF3IP3 | 2.474 | DISEASES 80705 | TSGA10 | 1.751 | DISEASES 10497 | UNC13B | 1.108 | DISEASES 2547 | XRCC6 | 1.866 | DISEASES 6935 | ZEB1 | 1.164 | DISEASES 7748 | ZNF195 | 2.228 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 846 |
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Disease | cutaneous t cell lymphoma |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:21) HP:0000989 | pruritis | 8 HP:0002664 | Neoplasia | 4 HP:0012190 | T cell lymphoma | 2 HP:0002665 | Lymphoma | 2 HP:0100827 | Lymphocytosis | 1 HP:0045029 | Eosinophilic fasciitis | 1 HP:0012490 | Inflammation of fat tissue | 1 HP:0002289 | Alopecia, complete | 1 HP:0002861 | Melanoma | 1 HP:0005550 | Chronic lymphatic leukemia | 1 HP:0003765 | Psoriasis | 1 HP:0001019 | Exfoliative dermititis | 1 HP:0012192 | Cutaneous T-cell lymphoma | 1 HP:0100537 | Inflammation of the fascia | 1 HP:0005523 | Lymphoproliferative disorder | 1 HP:0001635 | Congestive heart failure | 1 HP:0007431 | Congenital ichthyosis | 1 HP:0008064 | Ichthyosis | 1 HP:0001596 | Hair loss | 1 HP:0001045 | Blotchy loss of skin color | 1 HP:0002958 | Immune dysregulation | 1 |
Disease ID | 846 |
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Disease | cutaneous t cell lymphoma |
Manually Symptom | UMLS | Name(Total Manually Symptoms:15) C2364133 | infection C0702102 | arthritis mutilans C0343888 | cutaneous cryptococcosis C0162323 | polyarthritis C0085077 | sweet's syndrome C0037284 | skin lesions C0032285 | pneumoniae C0029166 | oral manifestations C0022504 | kaposi's varicelliform eruption C0020676 | hypothyroidism C0020097 | htlv-i C0017661 | iga nephropathy C0007682 | central nervous system disease C0007137 | squamous cell carcinoma C0003864 | arthritis |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:3) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 846 |
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Disease | cutaneous t cell lymphoma |
Case | (Waiting for update.) |